ライフサイエンスコーパス: lobed

1 nd leaf margin pattern (entire, serrated, or lobed).

2 eaf shape likely derived from a more complex lobed ancestral state that persists in extant Arabidopsi

3 on is spatially resolved and traces a double-lobed and axisymmetrical structure that is similar in mo

4 h from a simple polyhedral shape into highly lobed and interdigitated cells.

5 associated with the developing genitalia of lobed and non-lobed species.

6 DENND1B-S is bi-lobed, and interactions with Rab35 are through conserved

7 hipod Paraphronima gracilis has a pair of bi-lobed apposition compound eyes, each with a large upward

8 The pinnately lobed Aptian leaf fossil Mesodescolea plicata was origin

9 ilizes the PAZ-N domain, resulting in a "uni-lobed" architecture, which might facilitate the multi-tu

10 al outline that possesses a distinctly three lobed axis with an elevated central ridge and regularly

11 shape of patchy prisms is varied from small lobed, big lobed, trefoil, T-shaped to a reuleaux triang

12 actinomycetemcomitans developed asymmetric, lobed biofilm colonies that displayed complex architectu

13 n Patagonia, featuring highly inflated, five-lobed calyces, as a newly identified species of the deri

14 The cellular and molecular control of a lobed cell morphology is currently thought to involve PI

15 the transition from simple cell geometry to lobed cells.

16 The mushroom bodies are prominent lobed centers in the forebrain, or protocerebrum, of mos

17 ies that have undergone evolved loss, paired lobed centers referred to as "mushroom bodies" occur acr

18 s lead to a model for the development of the lobed chlamydial inclusion.

19 The EJC core is a four-lobed complex with a central channel and dimensions cons

20 plex geometries, including faceted and multi-lobed configurations.

21 ne in the organization of actin filaments in lobed cotyledon pavement cells and the highly elongated

22 reveals that a strain lacking BdpA produces lobed, disordered OMEs rather than membrane tubules or n

23 The binding cavities are two lobed, exhibiting two opposing pockets, each lined with

24 logical data indicate that digits emerged in lobed fins of early tetrapods, which were polydactylous.

25 ng ray-finned fish, regenerates its pectoral lobed fins with a remarkable accuracy.

26 ntal genes such as hoxc13 and sall1 in their lobed fins.

27 e of the ABC transporter BtuCD, reveals a bi-lobed fold resembling that of the ferrichrome binding pr

28 tion in grape leaves, which within a palmate-lobed framework exhibit diverse patterns of blade outgro

29 e prevents the nucleus, which becomes highly lobed, from physically blocking the intracellular bridge

30 raging of the tail fiber maps revealed a two-lobed globular structure at the distal end of each long

31 Lobed inclusions developed in cells infected at very low

32 The mushroom bodies of the insect brain are lobed integration centers made up of tens of thousands o

33 the most primitive known seeds, with highly lobed integument and exposed nucellus.

34 larities identified between the Genomosperma lobed integument and floral organs, we propose that the

35 he prominent phenotype of the ago7 mutant is lobed leaf margins and more widely spaced lateral organs

36 We demonstrate that lobed leaf morphology is produced in a dose-dependent ma

37 nt, as breeders have selected for entire and lobed leaf morphs resulting from a single locus, okra (l

38 a role for the gene in patterning the highly lobed leaf of the poppy.

39 pression of PALM1 effectively suppresses the lobed leaf phenotype from overexpression of a class 1 KN

40 We characterized the developmental roles of lobed leaflet1 by analyzing a recessive mutant in the mo

41 bidopsis thaliana argonaute7 (AGO7), Mt-AGO7/lobed leaflet1, is required for the biogenesis of a tran

42 produces a variety of phenotypes, including lobed leaves and ectopic stipules and meristems in the s

43 The shootlike features of the lobed leaves are consistent with the normal domain of KN

44 the stage of leaf development that produces lobed leaves in response to KN1.

45 Lobed leaves may be a labile intermediate step between d

46 loss of function and consequently converted lobed leaves to non-lobed leaves, as exhibited by most l

47 function in Arabidopsis results in rounded, lobed leaves with shorter and wider petioles, overexpres

48 d consequently converted lobed leaves to non-lobed leaves, as exhibited by most lettuce cultivars.

49 symmetric1 (as1) or asymmetric2 (as2) showed lobed leaves, ectopic stipules in the sinuses and defect

50 omologous landmarks in palmate, pinnate, and lobed leaves, using Cannabis as an example.

51 ower development; plants produce distinctive lobed leaves, with occasional ectopic meristems on the v

52 in Arabidopsis transforms simple leaves into lobed leaves.

53 ZFP) gene is required for the development of lobed leaves; a point mutation leads to its loss of func

54 These agonists bind to the receptor's bi-lobed ligand-binding domains (LBDs), which close around

55 When they are connected into lobed loops, where each fiber is geometrically constrain

56 ation showed that M. laxa colonies exhibited lobed margins and variable pigmentation, while M. fructi

57 A six-lobed membrane spanning cellulose synthesis complex (CSC

58 hibited classical Kranz anatomy with lightly lobed mesophyll cells having low chloroplast coverage.

59 sible transformation between four- and three-lobed molecules has been induced by current injection.

60 Furthermore, a triangular or tri-lobed morphology was clearly visualized in a subset of t

61 Their subunits contain a two-lobed N-terminal domain (NTD) that comprises over 40% of

62 g parameters uniquely inherent in the double-lobed nature of the Double-Helix Point Spread Function,

63 ocesses, presenting with unsegregated, multi-lobed nuclei caused by aberrant microtubule organization

64 o be either multinucleate or possessed multi-lobed nuclei that are normally located at the periphery

65 of individuals with SGD display atypical bi-lobed nuclei, lack expression of all secondary and terti

66 Paired lobed or dome-like neuropils characterize the first brai

67 re of the HeV N protein adopts the common bi-lobed paramyxoviral N protein fold; the N-terminal and C

68 scopy reconstructions show that eIF3, a five-lobed particle, interacts with the hepatitis C virus (HC

69 preading legionellae appear in an amorphous, lobed pattern that is most manifest at 25 to 30 degrees

70 In the leaf epidermis, intricately lobed pavement cells use Rho of plants (ROP) small GTPas

71 E1 assembles as a bi-lobed, presumably double hexameric structure on duplex D

72 ylogenetic context, we further show that the lobed primary plant bauplan is the evolutionary precurso

73 olecules of Cas1 (Cas2/32:Cas14) into a four-lobed propeller-shaped structure, where the two Cas2 dom

74 oordinated growth between interconnected and lobed regions of neighboring petal primordia, and betwee

75 ls, CSCs exist in the plasma membrane as six-lobed rosettes that contain at least three different cel

76 The two-lobed Rrp44 protein binds to the RNase PH domain side of

77 n and morphogenesis to its characteristic bi-lobed shape between the 2- and 3-fold stages of embryoge

78 ring and negative-staining EM revealed a two-lobed shape for VPS33B-VPS16B.

79 ic growth until development of the mature bi-lobed shape was completed.

80 Leaf epidermal cells have lobed shapes, which are thought to arise through a micro

81 Our data suggest that the two-lobed signal shape is also present in objects on the ord

82 th the developing genitalia of lobed and non-lobed species.

83 elopment, which results in young plants with lobed stem outlines and a discontinuous distribution of

84 We propose that the lobed structure is a result of division of inclusions oc

85 In the procyclic stage, a bi-lobed structure is found adjacent to the single ER exit

86 n ubiquitin ligase WWP1/AIP5 maintains a two-lobed structure like the HECT domain of the human ubiqui

87 ere, we found TbCentrin2 in an additional bi-lobed structure near to the Golgi apparatus.

88 w that, in the absence of ifenprodil, the bi-lobed structure of GluN2 ATD adopts an open conformation

89 Restriction of domain movement in the bi-lobed structure of the GluN2B ATD, by engineering of an

90 us outer capsid protein sigma3 reveals a two-lobed structure organized around a long central helix.

91 h only the first two subdomains of the three-lobed structure that is typical of canonical FERM domain

92 The development of this lobed structure was investigated in HeLa cells infected

93 r tandem beta-trefoil domains that form a bi-lobed structure with approximate pseudo 2-fold symmetry.

94 SmyD3 has a two-lobed structure with the substrate binding cleft located

95 itory aptamers analyzed have a predicted tri-lobed structure.

96 contrast to PIWI-clade Argonautes, the "uni-lobed" structure of the AGO complex makes multiple conta

97 specific inner and outer radii, or multiple lobed structures.

98 ion to study the development of these unique lobed structures.

99 d its A-type granules had a highly aberrant, lobed surface.

100 chemical vapor deposition (CVD) growth of 2-lobed symmetrical curvilinear graphene domains specifica

101 guing ripples and folds on the conspicuously lobed tips of their forewings.

102 is TAFs is largely consistent with the three-lobed topological map for yeast TFIID, which suggests th

103 atchy prisms is varied from small lobed, big lobed, trefoil, T-shaped to a reuleaux triangle by incre

104 The Mre11 dimer adopts a four-lobed U-shaped structure that is critical for proper MRN

105 Mesophyll cells were lobed where chloroplasts were located, facilitating cell